[Seminar/Training] China Medical Devices New China GMP Explanation Seminar
On October 6, local experts will explain the points of the new Chinese GMP compliance to be implemented in November 2026.
In November 2025, the revised "Good Manufacturing Practice (GMP) for Medical Devices" in China will be announced, and it is scheduled to be implemented in November 2026. Local experts will provide a clear explanation of the key points for compliance.
basic information
Date and Time: October 6, 2026 (Tuesday) 13:30 - 17:00 Venue: Online Seminar Topics: - Overview of China's new GMP - Differences from ISO 13485:2016 - New requirements that require particularly careful measures - Anticipated inspection styles Target Audience: Japanese manufacturers exporting medical devices and IVD products to China Application Method: Please apply through the seminar website.
Price information
42,000 yen (including tax for the text)
Price range
P2
Delivery Time
P1
Applications/Examples of results
We will welcome Chinese experts to clearly explain the key points regarding the revision of China's "Good Manufacturing Practice (GMP) for Medical Devices."
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TÜV SÜD is one of the world's largest third-party testing and certification organizations headquartered in Germany, providing certification, inspection, testing, and evaluation services across a wide range of fields. The company's Japanese subsidiary, TÜV SÜD Japan, was established in 1993 to respond to the growing demand for quality and safety testing and certification in the Japanese market under TÜV SÜD's business framework. It offers various testing, certification, auditing, management system certification, and training services in a wide range of fields, including electrical and electronic equipment, healthcare and medical devices, industrial equipment, IT and AV equipment, 5G-related devices, food, automotive, railways, energy and plant equipment, chemicals and processes, and cosmetics.